As clinical testing shifts away from targeted sequencing and WES, high-accuracy, cost-effective Whole Genome Sequencing (WGS) has emerged as the new gold standard.
In this webinar, we deep dive into how integrated genomic and transcriptomic workflows are improving diagnostic yields in prenatal and somatic testing, and how the ultra-high throughput sequencer DNBSEQ-T7+ is making the $100 genome a scalable reality.
Agenda:
Genome and Transcriptome Sequencing for Constitutional and Somatic Diagnoses
Peter Nagy, Chief Medical Officer, Praxis Genomics
Scaling the $100 Genome: Maximizing Throughput and Accuracy with the DNBSEQ-T7+
David Du, Director of Product Management, Complete Genomics
